Abstract | BACKGROUND:
TT-232, a somatostatin analogue, induces apoptosis in various tumours. The aim of our study was to characterise its effect on human melanoma cells and tumours. MATERIALS AND METHODS: Proliferation of seven melanoma cell lines was tested in vitro with the methylene blue test. D10 and 205 cells were also implanted into CB17-scid mice which received 30-150-750 micrograms/kg/day of TT-232 or saline. Animals with 205 cells received twice-daily subcutaneous injections whereas animals with D10 cells were treated with osmotic mini-pumps. In addition, TT-232 metabolites were generated with tissue homogenates and tested in vitro. RESULTS:
TT-232 strongly inhibited proliferation of all cell lines in vitro and tumour growth in vivo. Two out of 8 animals (30-150 micrograms/kg) in the 205 model and one out of 8(150 micrograms/kg) in the D10 model became completely tumour-free at the 11th and 9th day of treatment, respectively. TT-232 was degraded only by liver homogenate whilst its metabolite had no antiproliferative effect in vitro. CONCLUSIONS:
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Authors | R E Schwab, S Froidevaux, S Paku, M Tejeda, B Szende, A Pap, C Beglinger, A N Eberle, G Kéri |
Journal | Anticancer research
(Anticancer Res)
2001 Jan-Feb
Vol. 21
Issue 1A
Pg. 71-5
ISSN: 0250-7005 [Print] Greece |
PMID | 11299792
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antineoplastic Agents
- Peptides, Cyclic
- TT2-32
- Somatostatin
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Topics |
- Animals
- Antineoplastic Agents
(pharmacokinetics, pharmacology, therapeutic use)
- Cell Division
(drug effects)
- Chromatography, High Pressure Liquid
- Drug Screening Assays, Antitumor
- Female
- Humans
- Melanoma
(drug therapy, pathology)
- Mice
- Mice, SCID
- Peptides, Cyclic
(pharmacokinetics, pharmacology, therapeutic use)
- Somatostatin
(analogs & derivatives)
- Tumor Cells, Cultured
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